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HormoNet:一种用于激素-药物相互作用预测的深度学习方法。

HormoNet: a deep learning approach for hormone-drug interaction prediction.

机构信息

Department of Health Information Technology, School of Management and Medical Informatics, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

BMC Bioinformatics. 2024 Feb 28;25(1):87. doi: 10.1186/s12859-024-05708-7.

DOI:10.1186/s12859-024-05708-7
PMID:38418979
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10903040/
Abstract

Several experimental evidences have shown that the human endogenous hormones can interact with drugs in many ways and affect drug efficacy. The hormone drug interactions (HDI) are essential for drug treatment and precision medicine; therefore, it is essential to understand the hormone-drug associations. Here, we present HormoNet to predict the HDI pairs and their risk level by integrating features derived from hormone and drug target proteins. To the best of our knowledge, this is one of the first attempts to employ deep learning approach for prediction of HDI prediction. Amino acid composition and pseudo amino acid composition were applied to represent target information using 30 physicochemical and conformational properties of the proteins. To handle the imbalance problem in the data, we applied synthetic minority over-sampling technique technique. Additionally, we constructed novel datasets for HDI prediction and the risk level of their interaction. HormoNet achieved high performance on our constructed hormone-drug benchmark datasets. The results provide insights into the understanding of the relationship between hormone and a drug, and indicate the potential benefit of reducing risk levels of interactions in designing more effective therapies for patients in drug treatments. Our benchmark datasets and the source codes for HormoNet are available in: https://github.com/EmamiNeda/HormoNet .

摘要

已有多项实验证据表明,人体内源性激素可以通过多种方式与药物相互作用,从而影响药物疗效。激素药物相互作用(HDI)对药物治疗和精准医疗至关重要;因此,了解激素-药物的相互关系至关重要。在这里,我们提出了 HormoNet,通过整合源自激素和药物靶蛋白的特征来预测 HDI 对及其风险水平。据我们所知,这是首次尝试使用深度学习方法进行 HDI 预测。氨基酸组成和伪氨基酸组成被应用于使用蛋白质的 30 种物理化学和构象特性来表示靶标信息。为了解决数据中的不平衡问题,我们应用了合成少数过采样技术。此外,我们构建了用于 HDI 预测及其相互作用风险水平的新型数据集。HormoNet 在我们构建的激素-药物基准数据集上取得了优异的性能。研究结果深入了解了激素与药物之间的关系,并表明在设计针对患者的更有效的治疗方法时,降低相互作用风险水平具有潜在益处。我们的基准数据集和 HormoNet 的源代码可在:https://github.com/EmamiNeda/HormoNet 上获得。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3b2/10903040/13d7566e6a7b/12859_2024_5708_Fig7_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3b2/10903040/13d7566e6a7b/12859_2024_5708_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3b2/10903040/db3cf345c6d8/12859_2024_5708_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3b2/10903040/57b083e4c4c8/12859_2024_5708_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3b2/10903040/d58d29af0d63/12859_2024_5708_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3b2/10903040/715d03d1d444/12859_2024_5708_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3b2/10903040/22745430baa4/12859_2024_5708_Fig5_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3b2/10903040/13d7566e6a7b/12859_2024_5708_Fig7_HTML.jpg

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